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FDA 510(k)

TRI-PHASIX CHROMATIC ALGINATE

K-Number: K962741 · 1996-09-06

ApplicantParkell, Inc.
Decision Date1996-09-06
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TRI-PHASIX CHROMATIC ALGINATE is the device name listed in this FDA 510(k) record. The listed applicant is Parkell, Inc.. It received FDA 510(k) clearance on 1996-09-06 under 510(k) number K962741. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRI-PHASIX CHROMATIC ALGINATE?

TRI-PHASIX CHROMATIC ALGINATE is a medical device that received FDA 510(k) clearance on 1996-09-06. The listed applicant is Parkell, Inc.. The 510(k) number is K962741.

When did TRI-PHASIX CHROMATIC ALGINATE receive FDA 510(k) clearance?

TRI-PHASIX CHROMATIC ALGINATE received FDA 510(k) clearance on 1996-09-06, under 510(k) number K962741.

Who is the listed applicant for TRI-PHASIX CHROMATIC ALGINATE?

The FDA 510(k) record lists Parkell, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRI-PHASIX CHROMATIC ALGINATE?

The FDA product code for TRI-PHASIX CHROMATIC ALGINATE is ELW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Parkell, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: ELW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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